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rs766305807

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766305807(C;T)
Make rs766305807(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position101304267
GeneIMPG2
is asnp
is mentioned by
dbSNPrs766305807
ebirs766305807
HLIrs766305807
Exacrs766305807
Varsomers766305807
Maprs766305807
PheGenIrs766305807
hapmaprs766305807
1000 genomesrs766305807
hgdprs766305807
ensemblrs766305807
gopubmedrs766305807
geneviewrs766305807
scholarrs766305807
googlers766305807
pharmgkbrs766305807
gwascentralrs766305807
openSNPrs766305807
23andMers766305807
23andMe allrs766305807
SNP Nexus

SNPshotrs766305807
SNPdbers766305807
MSV3drs766305807
GWAS Ctlgrs766305807
Max Magnitude0
ClinVar
Risk rs766305807(T;T)
Alt rs766305807(T;T)
Reference rs766305807(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IMPG2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.101023111C>G
CLNSRC
CLNACC RCV000171368.1,